(Q28214777)

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N Avidan

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T Potikha

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H Hochner

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M Chen

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T Olender

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M Shemesh

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M Sadeh

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G Grabov-Nardini

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I Shmilevich

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A Friedmann

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G Karpati

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W G Bradley

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L Baumbach

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E B Asher

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J S Beckmann

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Z Argov

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S Mitrani-Rosenbaum

Inclusion body myositis and myopathies

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language of work or name

English

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publication date

September 2001

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83-7

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cites work

1 reference

7 January 2021

"Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews

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7 January 2021

Fine-structure mapping of the hereditary inclusion body myopathy locus

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7 January 2021

Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13

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7 January 2021

Chromosomal location and some structural features of human clathrin light-chain genes (CLTA and CLTB)

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7 January 2021

Regulation of matrix metalloproteinase-9 and inhibition of tumor invasion by the membrane-anchored glycoprotein RECK

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7 January 2021

A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Purification and characterization of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase

1 reference

7 January 2021

Mutations in the human UDP-N-acetylglucosamine 2-epimerase gene define the disease sialuria and the allosteric site of the enzyme

1 reference

7 January 2021

A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Molecular cloning and functional expression of UDP-N-acetyl-glucosamine 2-epimerase/N-acetylmannosamine kinase

1 reference

7 January 2021

Selective loss of either the epimerase or kinase activity of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase due to site-directed mutagenesis based on sequence alignments

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7 January 2021

Microbial genes in the human genome: lateral transfer or gene loss?

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7 January 2021

UDP-GlcNAc 2-epimerase: a regulator of cell surface sialylation

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7 January 2021

Initial sequencing and analysis of the human genome

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7 January 2021

What If There Are Only 30,000 Human Genes?

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7 January 2021

Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation

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7 January 2021

Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9

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7 January 2021

Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: current concepts of diagnosis and pathogenesis

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7 January 2021

Genetics of inclusion body myopathies

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7 January 2021

Hereditary inclusion body myopathy maps to chromosome 9p1-q1

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7 January 2021

Oligosaccharides in urine of patients with glycoprotein storage diseases. I. Rapid detection by thin-layer chromatography

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7 January 2021

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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7 January 2021

Using CLUSTAL for multiple sequence alignments

1 reference

7 January 2021